Nakamura N
Acta Pathol Jpn. 1986 May;36(5):641-64. doi: 10.1111/j.1440-1827.1986.tb01054.x.
A clinicopathological investigation was made on 15 autopsy cases with allogeneic bone marrow transplantation. Engraftment was recognized in 11 patients, 6 out of which survived more than 100 days postgrafting, and 5 terminated within 100 days. The other patients succumbed to sepsis before engraftment. In 8 evaluated cases with clinical acute graft versus host disease (GVHD), involvement of acute GVHD was histologically confirmed in the skin, liver, and/or intestine. Atypical ductal changes similar to those of interlobular bile ducts were noted in the pancreas and esophageal gland in a patient with severe acute GVHD. Although 6 long-term patients showed neither definite lichenoid papulae nor sicca syndrome diagnostic for clinical chronic GVHD, 4 patients exhibited prolonged hepatic dysfunction and/or abnormal serological tests suggestive of autoimmunity, and they had some degree of basal vacuolar degeneration with or without lymphocytic infiltrates in the dermis, and atypical degeneration of small bile ducts at the same level as seen in acute GVHD ranging 20 to 50 micron in diameter. Chronic sialoadenitis with atypical epithelial degeneration was evident in two of them. A major cause of death was interstitial pneumonia of viral or fungal etiology due to persistent immunodeficiency.
对15例同种异体骨髓移植尸检病例进行了临床病理研究。11例患者出现植入,其中6例在移植后存活超过100天,5例在100天内死亡。其他患者在植入前死于败血症。在8例评估为临床急性移植物抗宿主病(GVHD)的病例中,皮肤、肝脏和/或肠道的急性GVHD累及在组织学上得到证实。一名严重急性GVHD患者的胰腺和食管腺中发现了类似于小叶间胆管的非典型导管改变。虽然6例长期存活患者既无明确的苔藓样丘疹,也无临床慢性GVHD诊断所依据的干燥综合征,但4例患者出现了肝功能长期异常和/或提示自身免疫的血清学检查异常,他们有一定程度的基底空泡变性,真皮有或无淋巴细胞浸润,以及与急性GVHD相同水平的小胆管非典型变性,直径为20至50微米。其中2例有明显的慢性涎腺炎伴非典型上皮变性。主要死亡原因是由于持续免疫缺陷导致的病毒或真菌性间质性肺炎。